Visible Light‐Driven Photoredox Synthesis of Sulfonylated Benzimidazoisoquinolines via 10 <i>H</i> ‐Phenothiazine‐Catalyzed Electron Donor–Acceptor Complexes

An unmodified 10 H ‐phenothiazine is directly utilized as an efficient photocatalyst to enable ready access to sulfonylated benzo[4,5]imidazo[2,1‐ a ]isoquinoline derivatives from N ‐allyl benzimidazoles and sulfonyl chlorides. The reaction involves the formation of electron donor–acceptor complexes between phenothiazine and sulfonyl chloride, which, upon visible light irradiation, undergo single‐electron transfer to generate sulfonyl radicals. The reaction features mild conditions, broad substrate scope, and high efficiency.

Authors

Institutions

Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-06-12
DOI
https://doi.org/10.1002/adsc.9581
Citations
2
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
1.87

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Visible Light‐Driven Photoredox Synthesis of Sulfonylated Benzimidazoisoquinolines via 10 H ‐Phenothiazine‐Catalyzed Electron Donor–Acceptor Complexes

Ningning Li, Cheng‐Liang Liu, Zhixing Liu, Yi Lv et al.
2 citations
Advanced Synthesis & Catalysis
Sulfur-Based Synthesis Techniques
1.87
article

Visible Light‐Driven Photoredox Synthesis of Sulfonylated Benzimidazoisoquinolines via 10 H ‐Phenothiazine‐Catalyzed Electron Donor–Acceptor Complexes

Ningning Li, Cheng‐Liang Liu, Zhixing Liu, Yi Lv, Jiang‐Sheng Li, He Li, Chenxi Zhang, Zhiwei Li, Hanwen Liu, Zi‐Rui Kuang
article en
2 citations

Abstract

An unmodified 10 H ‐phenothiazine is directly utilized as an efficient photocatalyst to enable ready access to sulfonylated benzo[4,5]imidazo[2,1‐ a ]isoquinoline derivatives from N ‐allyl benzimidazoles and sulfonyl chlorides. The reaction involves the formation of electron donor–acceptor complexes between phenothiazine and sulfonyl chloride, which, upon visible light irradiation, undergo single‐electron transfer to generate sulfonyl radicals. The reaction features mild conditions, broad substrate scope, and high efficiency.

Advanced Synthesis & CatalysisVol. 367(14)
Changsha University of Science and Technology (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hunan Province, Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation, Changsha University of Science and Technology
Openalex Percentile: Top 15%
Sulfur-Based Synthesis Techniques
1.87
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.